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TCL1B TCL1 family AKT coactivator B [ Homo sapiens (human) ]

Gene ID: 9623, updated on 23-Nov-2021

Summary

Official Symbol
TCL1Bprovided by HGNC
Official Full Name
TCL1 family AKT coactivator Bprovided by HGNC
Primary source
HGNC:HGNC:11649
See related
Ensembl:ENSG00000213231 MIM:603769
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TML1; SYN-1
Expression
Biased expression in testis (RPKM 1.5), lymph node (RPKM 1.2) and 6 other tissues See more
Orthologs
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Genomic context

See TCL1B in Genome Data Viewer
Location:
14q32.13
Exon count:
4
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (95686426..95692628)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (96152763..96158965)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370643 Neighboring gene T cell leukemia/lymphoma 6 Neighboring gene TCL1 family AKT coactivator A Neighboring gene uncharacterized LOC107984703

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Potential readthrough

Included gene: TCL6

Homology

General protein information

Preferred Names
T-cell leukemia/lymphoma protein 1B
Names
T cell leukemia/lymphoma 1B
T-cell lymphoma/leukemia 1B
TCL1/ MTCP1-like 1
oncogene TCL-1B
syncytiotrophoblast-specific protein

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_004918.4NP_004909.1  T-cell leukemia/lymphoma protein 1B

    See identical proteins and their annotated locations for NP_004909.1

    Status: VALIDATED

    Source sequence(s)
    AF137027, BC051000
    Consensus CDS
    CCDS32151.1
    UniProtKB/Swiss-Prot
    O95988
    UniProtKB/TrEMBL
    A0A024R6P4
    Related
    ENSP00000343223.6, ENST00000340722.8
    Conserved Domains (1) summary
    pfam01840
    Location:1124
    TCL1_MTCP1; TCL1/MTCP1 family

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    95686426..95692628
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_199206.2: Suppressed sequence

    Description
    NM_199206.2: This RefSeq was permanently suppressed because it retains intronic sequence.
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